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  1. General Info
  2. Effects Info
  3. Reference
Drug Details
01. General Information
Name 2-methoxyestradiol
PubChem CID 66414
Molecular Weight 302.4g/mol
Synonyms

2-Methoxyestradiol, 362-07-2, Panzem, 2-Methoxyestradiol-17beta, 2-Hydroxyestradol 2-methyl ether, 2-ME2, 2ME2, 2-MeOE2, Estradiol, 2-methoxy-, 2-Methoxyestradiol (2-MeOE2), 2-methoxyoestradiol, 2-Hydroxyestradiol 2-methyl ether, 2-methoxy-17beta-estradiol, (17beta)-2-Methoxyestra-1,3,5(10)-triene-3,17-diol, NSC-659853, 2-Methoxyestra-1,3,5(10)-triene-3,17beta-diol, 2-Methoxy-estradiol, 2-Methoxy-beta-estradiol, MLS000028819, 6I2QW73SR5, CHEMBL299613, (8R,9S,13S,14S,17S)-2-methoxy-13-methyl-7,8,9,11,12,13,14,15,16,17-decahydro-6H-cyclopenta[a]phenanthrene-3,17-diol, CHEBI:28955, Estra-1,3,5(10)-triene-3,17-diol, 2-methoxy-, (17beta)-, Panzem NCD, 1,3,5(10)-ESTRATRIEN-2,3,17-BETA-TRIOL 2-METHYL ETHER, 2-methoxy-estra-1,3,5(10)-triene-3,17beta-diol, MFCD00010489, Estra-1,3,5(10)-triene-3,17beta-diol, 2-methoxy-, SMR000058478, 2-Methoxy 17b-Estradiol, 2-Methoxy 17beta-Estradiol, (17beta)-2-methoxyestra-1(10),2,4-triene-3,17-diol, PulmoLAR, 2-Methoxy-.beta.-estradiol, NSC 659853, UNII-6I2QW73SR5, CCRIS 9405, 1lhw, Opera_ID_634, Estra-1,3,5(10)-triene-3,17-diol, 2-methoxy-, (17b)-, 2-Methoxyestradiol Powder, 2-Methoxyestradiol, powder, 2-Methoxy 17?-Estradiol, M 6383, SCHEMBL8796, 2-MeO-E2, Lopac0_000739, (8R,9S,13S,14S,17S)-2-methoxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthrene-3,17-diol, MLS001076279, MLS006010142, 1,3,5(10)-Estratriene-2,3,17-triol 2-methyl ether, DTXSID3040938, GTPL12058, HMS2230L22, HMS3262C20, HMS3412H22, HMS3676H22, BCP02076, 2-METHOXYESTRADIOL [WHO-DD], 2-METHOXYOESTRADIOL [MART.], Tox21_500739, BDBM50060957, LMST02010035, s1233, AKOS015901723, 2-Methoxyestradiol, analytical standard, BCP9000109, CCG-204824, CS-0176, DB02342, LP00739, SDCCGSBI-0050717.P002, SMP2_000045, NCGC00094082-03, NCGC00094082-04, NCGC00094082-13, NCGC00261424-01, AC-32086, AS-19175, BP-25393, HY-12033, EU-0100739, FT-0612836, M2530, NS00115961, C05302, C74863, AB00639611-09, AB00639611_10, SR-01000076000, 2-methoxy-1,3,5 (10)-estratriene-3,17beta-diol, 2-Methoxyestra-1,3,5(10)-triene-3,17-diol #, Q4596897, SR-01000076000-1, BRD-K44408410-001-20-0, (17?)-2-Methoxyestra-1(10),2,4-triene-3,17-diol, 17beta-2-methoxyestra-1,3,5(10)-triene-3,17-diol, Estra-1,3,5(10)-triene-3,17.beta.-diol, 2-methoxy-, estra-1(10),2,4-triene-3,17-diol, 2-methoxy-, (17beta)-, (14beta,17beta)-2-methoxyestra-1(10),2,4-triene-3,17-diol, (17.BETA.)-2-METHOXYESTRA-1,3,5(10)-TRIENE-3,17-DIOL, B3C40B85-1733-48FE-8418-A39011910D19, Estra-1,3,5(10)-triene-3,17-diol, 2-methoxy-, (17.beta.)-

Drug Type Small molecule
Formula C₁₉H₂₆O₃
SMILES CC12CCC3C(C1CCC2O)CCC4=CC(=C(C=C34)OC)O
InChI 1S/C19H26O3/c1-19-8-7-12-13(15(19)5-6-18(19)21)4-3-11-9-16(20)17(22-2)10-14(11)12/h9-10,12-13,15,18,20-21H,3-8H2,1-2H3/t12-,13+,15-,18-,19-/m0/s1
InChIKey CQOQDQWUFQDJMK-SSTWWWIQSA-N
CAS Number 362-07-2
ChEMBL ID CHEMBL299613
ChEBI ID CHEBI:28955
TTD ID D06NYA
Drug Bank ID DB02342
KEGG ID C05302
Toxicity Organism Test Type Route(Dose)
rat LD50 intraperitoneal(165 mg/kg)
mouse LD50 intraperitoneal(254 mg/kg)
rat LD50 oral(322 mg/kg)
Structure 2D-img
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2D MOL 3D MOL
02. Combinatorial Therapeutic Effect(s)
Synergistic Effect
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Enhancing Drug Efficacy
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Combination Pair ID: 783
Pair Name Eugenol, 2-methoxyestradiol
Partner Name Eugenol
Disease Info [ICD-11: 2C82] Prostate cancer Investigative
Biological Phenomena Induction-->Blockade of cell cycle in G2/M phase
Gene Regulation Up-regulation Expression BAX hsa581
Down-regulation Expression BCL2 hsa596
In Vitro Model LNCaP Prostate carcinoma Homo sapiens (Human) CVCL_0395
PC-3 Prostate carcinoma Homo sapiens (Human) CVCL_0035
DU145 Prostate carcinoma Homo sapiens (Human) CVCL_0105
Result Combining these agents may allow ameliorating any adverse effects of either 2-ME(2) or eugenol alone by reducing their individual concentrations should these two agents be developed for human use.
03. Reference
No. Title Href
1 Combination of 2-methoxyestradiol (2-ME2) and eugenol for apoptosis induction synergistically in androgen independent prostate cancer cells. J Steroid Biochem Mol Biol. 2009 Jan;113(1-2):25-35. doi: 10.1016/j.jsbmb.2008.11.002. Click
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